Evidence map›Paper›PMID 25820824›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Interaction with CCNH/CDK7 facilitates CtBP2 promoting esophageal squamous cell carcinoma (ESCC) metastasis via upregulating epithelial-mesenchymal transition (EMT) progression.

Jianguo Zhang, Junya Zhu, Lei Yang, Chengqi Guan, Runzhou Ni, Yuchan Wang, Lili Ji, Ye Tian

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 29 citations in OpenAlex.

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  19. High expression of TRIM44 is associated with enhanced cell proliferation, migration, invasion, and resistance to doxorubicin in hepatocellular carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Jianguo ZhangDepartment of Oncology, The Second Affiliated Hospital, Soochow University, Suzhou, 215000, Jiangsu, China.
Junya ZhuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Lei YangDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Chengqi GuanDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Runzhou NiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Yuchan WangDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Lili JiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Ye TianDepartment of Oncology, The Second Affiliated Hospital, Soochow University, Suzhou, 215000, Jiangsu, China. tianye_2014@126.com.
Affiliated Hospital of Nantong University · CNNantong University · CNSecond Affiliated Hospital of Soochow University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CtBP2, as a transcriptional corepressor of epithelial-specific genes, has been reported to promote tumor due to upregulating epithelial-mesenchymal transition (EMT) in cancer cells. CtBP2 was also demonstrated to contribute to the proliferation of esophageal squamous cell carcinoma (ESCC) cells through a negative transcriptional regulation of p16(INK4A). In this study, for the first time, we reported that CtBP2 expression, along with CCNH/CDK7, was higher in ESCC tissues with lymph node metastases than in those without lymph node metastases. Moreover, both CtBP2 and CCNH/CDK7 were positively correlated with E-cadherin, tumor grade, and tumor metastasis. However, the concrete mechanism of CtBP2's role in enhancing ESCC migration remains incompletely understood. We confirmed that CCNH/CDK7 could directly interact with CtBP2 in ESCC cells in vivo and in vitro. Furthermore, our data demonstrate for the first time that CtBP2 enhanced the migration of ESCC cells in a CCNH/CDK7-dependent manner. Our results indicated that CCNH/CDK7-CtBP2 axis may augment ESCC cell migration, and targeting the interaction of both may provide a novel therapeutic target of ESCC.

Indexed as

AgedAlcohol OxidoreductasesCarcinoma, Squamous CellCell MovementCell ProliferationCo-Repressor ProteinsCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent KinasesCyclin HEpithelial-Mesenchymal TransitionEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaFemaleGene Expression Regulation, NeoplasticHumansAlcohol OxidoreductasesCCNH protein, humanCDK7 protein, humanCo-Repressor ProteinsCTBP2 protein, humanCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent KinasesCyclin HNerve Tissue ProteinsC-terminal binding protein 2 (CtBP2)Cyclin-dependent kinase 7 (CDK7)Cyclin H (CCNH)Epithelial-mesenchymal transition (EMT)Esophageal squamous cell carcinoma (ESCC)Metastasis

Identifiers

PMID25820824
OpenAlexW2094703974

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.